Descrizione del lavoro
Who we are looking forPurposeSupport the analytical activities required for producing information and documentation suitable for preclinical and clinical development, and registration of new Drug Substances, including starting materials and intermediates, with particular focus on risk quality management in accordance with GMP/cGMPMain Responsibilities• Supervise the testing activities on materials for non-clinical and clinical use• Study Monitor of analytical method development/validation/transfer studies• Study Monitor of stability studies• Study Monitor of Drug Substances characterization studies...